Medical Affairs Director Jobs

About The Position

Requirements

• At least 5 years of progressive experience in medical affairs, clinical development, or related roles.
• Demonstrated experience executing global or multi-regional medical activities.
• Strong scientific acumen and ability to interpret and communicate clinical data clearly and in a balanced manner.
• Ability to execute in a fast-paced, matrixed, global organization and coordinate multiple workstreams with strong attention to quality and timelines.
• Operational excellence, project-management discipline, and prioritization skills.
• Knowledge of medical governance, compliance, and quality standards for Medical Affairs activities.
• Excellent cross-functional collaboration skills and ability to influence in a matrix without direct authority.
• High standards of integrity and accountability, with a patient-centered mindset.

Nice To Haves

• Experience in hematology across the product lifecycle, including launch and lifecycle support, evidence generation, and scientific communications.

Responsibilities

• Execute assigned components of the integrated global medical plan for sonrotoclax and deliver tactics and deliverables on time and to a high standard.
• Translate global priorities into executable workstreams in partnership with regional medical teams, including content packages, training toolkits, and congress deliverables.
• Track execution progress, risks, and dependencies; escalate issues and propose mitigation plans to GMA leadership.
• Support scientific exchange with key opinion leaders, academic institutions, cooperative groups, and professional societies in alignment with global medical priorities.
• Execute global and/or regional advisory boards, including defining objectives and agendas, developing materials, capturing insights, and producing post-meeting outputs.
• Capture, synthesize, and communicate actionable insights from external interactions to inform medical execution and cross-functional alignment.
• Support execution of the Integrated Evidence Plan and its initiatives.
• Support concept and protocol reviews and evidence-gap assessment for assigned therapeutic areas.
• Coordinate with internal and external partners, including CROs, vendors, and investigators, to ensure studies meet timeline, quality, and compliance expectations.
• Execute scientific tactics and deliverables for hematology congresses such as ASH, EHA, and ASCO, and for peer-reviewed journals.
• Support congress planning and execution, including data review meetings, medical booth or medical affairs station support, scientific narrative consistency, and internal readiness.
• Ensure scientific accuracy, balance, and consistency across global and regional scientific materials.
• Collaborate with Clinical Development, Regulatory, Safety, Market Access/HEOR, and Commercial teams while maintaining appropriate medical-commercial separation.
• Support regional and affiliate medical teams with aligned content, scientific updates, and execution toolkits, enabling a consistent global scientific narrative across geographies.
• Manage assigned budgets for medical activities and vendors, promote efficient resource use, and coordinate timely purchase orders and contracts with operations.
• Coordinate with agencies and vendors, including medical communications, digital, and congress logistics providers, to deliver high-quality outputs on schedule.

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• 401(k)
• FSA/HSA
• Life insurance
• Paid time off
• Wellness program
• Annual bonus plan eligibility for non-commercial roles
• Incentive compensation plan eligibility for commercial roles
• Eligibility for discretionary equity awards
• Voluntary Employee Stock Purchase Plan